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  1. AU="Yom, Jina"
  2. AU="Sue Casey"
  3. AU="Arimura, Takashi"
  4. AU="Kizilkilic, Osman"

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  1. Artikel ; Online: AGS3 antagonizes LGN to balance oriented cell divisions and cell fate choices in mammalian epidermis.

    Descovich, Carlos P / Lough, Kendall J / Jena, Akankshya / Wu, Jessica J / Yom, Jina / Spitzer, Danielle C / Uppalapati, Manuela / Kedziora, Katarzyna M / Williams, Scott E

    eLife

    2023  Band 12

    Abstract: Oriented cell divisions balance self-renewal and differentiation in stratified epithelia such as the skin epidermis. During peak epidermal stratification, the distribution of division angles among basal keratinocyte progenitors is bimodal, with planar ... ...

    Abstract Oriented cell divisions balance self-renewal and differentiation in stratified epithelia such as the skin epidermis. During peak epidermal stratification, the distribution of division angles among basal keratinocyte progenitors is bimodal, with planar and perpendicular divisions driving symmetric and asymmetric daughter cell fates, respectively. An apically restricted, evolutionarily conserved spindle orientation complex that includes the scaffolding protein LGN/Pins/Gpsm2 plays a central role in promoting perpendicular divisions and stratification, but why only a subset of cell polarize LGN is not known. Here, we demonstrate that the LGN paralog, AGS3/Gpsm1, is a novel negative regulator of LGN and inhibits perpendicular divisions. Static and ex vivo live imaging reveal that AGS3 overexpression displaces LGN from the apical cortex and increases planar orientations, while AGS3 loss prolongs cortical LGN localization and leads to a perpendicular orientation bias. Genetic epistasis experiments in double mutants confirm that AGS3 operates through LGN. Finally, clonal lineage tracing shows that LGN and AGS3 promote asymmetric and symmetric fates, respectively, while also influencing differentiation through delamination. Collectively, these studies shed new light on how spindle orientation influences epidermal stratification.
    Mesh-Begriff(e) Animals ; Cell Cycle Proteins/metabolism ; Carrier Proteins/metabolism ; Cell Division ; Epidermis/metabolism ; Cell Differentiation/genetics ; Spindle Apparatus/metabolism ; Cell Polarity ; Mammals/metabolism
    Chemische Substanzen Cell Cycle Proteins ; Carrier Proteins
    Sprache Englisch
    Erscheinungsdatum 2023-04-05
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.80403
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome.

    Mattis, Joanna / Somarowthu, Ala / Goff, Kevin M / Jiang, Evan / Yom, Jina / Sotuyo, Nathaniel / Mcgarry, Laura M / Feng, Huijie / Kaneko, Keisuke / Goldberg, Ethan M

    eLife

    2022  Band 11

    Abstract: Dravet syndrome (DS) is a neurodevelopmental disorder due to pathogenic variants ... ...

    Abstract Dravet syndrome (DS) is a neurodevelopmental disorder due to pathogenic variants in
    Mesh-Begriff(e) Animals ; Autism Spectrum Disorder ; Disease Models, Animal ; Epilepsies, Myoclonic ; Epileptic Syndromes ; Interneurons/physiology ; Mice ; NAV1.1 Voltage-Gated Sodium Channel/genetics ; Seizures/genetics ; Spasms, Infantile
    Chemische Substanzen NAV1.1 Voltage-Gated Sodium Channel ; Scn1a protein, mouse
    Sprache Englisch
    Erscheinungsdatum 2022-02-25
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.69293
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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